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Identification of Modifying Genes Associated with Fragile X Disorders Using TWAS
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Uncovering the contribution of rare genetic variants in orofacial clefts
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The Epigenetics of Aging: Exploring Biomarkers and the Interplay Within the Aging Epigenome
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Genetic variation in Down syndrome associated congenital heart
defects
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Serum Dopamine Beta Hydroxylase (DβH) enzyme activity
changes within individual women according to stage of pregnancy:
Evidence that regulation of expression of DβH differs during
pregnancy in women carrying different genotypes at rs1611115.
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Genomics of Down Syndrome Associated Congenital Heart Defects
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Development of Novel Analytic Methods for Improved Gene Mapping of Complex Human Traits
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Genetic epidemiology of phenotypes associated with FMR1premutation alleles
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Genetic and environmental contributions to gastrointestinal health
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Genetic Variation in Recombination as a Risk Factor for
Nondisjunction
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